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70758-62-2

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70758-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70758-62-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,5 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70758-62:
(7*7)+(6*0)+(5*7)+(4*5)+(3*8)+(2*6)+(1*2)=142
142 % 10 = 2
So 70758-62-2 is a valid CAS Registry Number.

70758-62-2Relevant academic research and scientific papers

Synthesis of 1,3-diaryl-spiro[azetidine-2,3′-indoline]-2′,4-diones: Via the Staudinger reaction: Cis - Or trans -diastereoselectivity with different addition modes

Beloglazkina, Elena,Filatov, Vadim,Kukushkin, Maksim,Kuznetsova, Juliana,Majouga, Alexander,Skvortsov, Dmitry,Tafeenko, Viktor,Zyk, Nikolay

, p. 14122 - 14133 (2020/04/23)

A new synthetic approach for realizing biologically relevant bis-aryl spiro[azetidine-2,3′-indoline]-2′,4-diones was developed based on Staudinger ketene-imine cycloaddition through the one-pot reaction of substituted acetic acids and Schiff bases in the presence of oxalyl chloride and an organic base. A series of [azetidine-2,3′-indoline]-2′,4-diones were synthesized using this method. For comparison, the same compounds were obtained using a known technique, where ketene is generated from pre-synthesized acyl chloride. It was shown that the use of oxalyl chloride for ketene generation in the one-pot reaction at room temperature allows for the reversal of the diastereoselectivity of spiro-lactam formation, unlike previously described procedures.

Tin powder-promoted one-pot synthesis of 3-spiro-fused or 3,3′-disubstituted 2-oxindoles

Wang, Juanjuan,Huang, Danfeng,Wang, Ke-Hu,Peng, Xiansha,Su, Yingpeng,Hu, Yulai,Fu, Ying

supporting information, p. 9533 - 9542 (2016/10/22)

A convenient and efficient method for the constructions of 3-spirooxindole derivatives or 3,3′-disubstituted oxindoles has been developed from one-pot reactions of isatins, hydrazides or aromatic amines, 2-(bromomethyl)acrylic ester and tin powder in the

Synthesis and biological study of novel indole-3-imine-2-on derivatives as src kinase and glutathione S-transferase inhibitors

Kurt, Z. Kilic,Aydin,Isgoer,Isgoer,Olgen

, p. 19 - 26 (2013/08/22)

The aim of this study is to design and synthesize novel dual inhibitors of Src protein tyrosine kinase (PTK) and Glutathione S-transferases (GSTs), as a potential drug lead with therapeutic efficacy on cancer and immune disorders. The biological activity

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